Identity
- Trade Name
- Gumové škrtidlo EUDAMED
- Device Name
- Obinadlo škrticí pryžové EUDAMED
- Model / Reference
- 1398 EUDAMED1532 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08595154107245 EUDAMED08595154107139 EUDAMED
- Basic UDI-DI
- 85951541013VD EUDAMED
- EMDN Code
- V9003 TOURNIQUETS EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Czechia EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Gumové škrtidlo by STERIWUND spol. s r.o. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 85951541013VD | Class I | Active |
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Manufacturer
- Manufacturer
- STERIWUND spol. s r.o.
- EUDAMED SRN
- CZ-MF-000036963
Sources (2)
- EUDAMED 19eefba0-e998-40c9-9487-430d00502331 61 fields · synced Jul 13, 2026
- EUDAMED 743fb9ef-0732-4123-a396-621a21d99bc1 61 fields · synced May 17, 2026